chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5160721673160721673AA44GENIChomozygous141691958
5160722599160722600CG53GENIChomozygous146789926
5160723283160723283AGCTCACA50GENIChomozygous141691959
5160723736160723748ACGGGTGTCTTA61GENIChomozygous141691960
5160725169160725170AG53GENIChomozygous141769997
5160723737160723738CT61GENICheterozygous154256429
5160724742160724743CA24GENIChomozygous154256431
5160722829160722830GA48GENIChomozygous141769990
5160723979160723980AG36GENIChomozygous141769991
5160724220160724221CT57GENIChomozygous141769992
5160724483160724484CT53GENIChomozygous141769993
5160724634160724635AC36GENIChomozygous141769994
5160724909160724910CT41GENIChomozygous141769995
5160725147160725148TC57GENIChomozygous141769996
5160723737160723738C61GENIChomozygous403164600
5160724805160724806TC28GENIChomozygous144363598
5160725031160725031CATTAGAGCCAGCCAA38GENICpossibly homozygous146772295
5160725373160725374GA46GENICpossibly homozygous141769998
5160726369160726370GT66GENIChomozygous141769999
5160727093160727094TC70GENIChomozygous141770000
5160727598160727600TT53GENIChomozygous141691961
5160727816160727817CT61GENIChomozygous141770002
5160727836160727837GA59GENIChomozygous141770003
5160728769160728770GT56GENIChomozygous141770004
5160728772160728773AC54GENIChomozygous141770005
5160729248160729249GA69GENIChomozygous141770006
5160729536160729537GA62GENIChomozygous141770007
5160730480160730480TCT49GENIChomozygous141691963
5160731229160731230CT64GENIChomozygous141770008